Alopecia, congenital

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Congenital alopecia [OMIM:Congenital alopecia]
Quality:
Cross references:
OMIM: "Alopecia, congenital" [OMIM:Alopecia, congenital]
OMIM: "Congenital alopecia" [OMIM:Congenital alopecia]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant palmoplantar keratoderma and congenital alopecia (Orphanet:1010)
Severe T-cell immunodeficiency - congenital alopecia - nail dystrophy (Orphanet:169095)